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Disease association ontology term - MONDO:0008379 - retinitis pigmentosa 10

Term summary

ID
MONDO:0008379
Name
retinitis pigmentosa 10
Ontology or CV name
Disease association
Definition
Any retinitis pigmentosa in which the cause of the disease is a mutation in the IMPDH1 gene.

Parents

Annotation

Disease association

MONDO:0008379 - retinitis pigmentosa 10

References:

Genes: